Canonical Allele Identifier: CA352728794

Gene: NDUFAF3

Linked Data

• MyVariant Identifiers: chr3:g.49059970A>C (hg19) ; chr3:g.49022537A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.49022537A>C , CM000665.2:g.49022537A>C	GRCh38
NC_000003.11:g.49059970A>C , CM000665.1:g.49059970A>C	GRCh37
NC_000003.10:g.49034974A>C	NCBI36
NG_012091.1:g.11906T>G
NG_016282.1:g.7063A>C
NG_033126.1:g.3535T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326925.11:c.269A>C MANE Select	ENSP00000323076.5:p.Asn90Thr
ENST00000326912.8:c.98A>C	ENSP00000323003.4:p.Asn33Thr
ENST00000326925.10:c.269A>C	ENSP00000323076.5:p.Asn90Thr
ENST00000395458.6:c.98A>C	ENSP00000378843.2:p.Asn33Thr
ENST00000451378.2:c.98A>C	ENSP00000402465.2:p.Asn33Thr
ENST00000480392.1:n.293A>C
ENST00000496152.1:n.425A>C
NM_199069.1:c.269A>C	NP_951032.1:p.Asn90Thr
NM_199070.1:c.98A>C	NP_951033.1:p.Asn33Thr
NM_199073.1:c.98A>C	NP_951047.1:p.Asn33Thr
NM_199074.1:c.98A>C	NP_951056.1:p.Asn33Thr
NM_199069.2:c.269A>C MANE Select	NP_951032.1:p.Asn90Thr
NM_199070.2:c.98A>C	NP_951033.1:p.Asn33Thr
NM_199073.2:c.98A>C	NP_951047.1:p.Asn33Thr
NM_199074.2:c.98A>C	NP_951056.1:p.Asn33Thr